RAG2 Gene Omenn Syndrome Genetic Test
Test Components
Price: 4400.0 AED
Sample Condition
Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery
3 to 4 Weeks
Method
NGS Technology
Test Type
Osteology Dermatology Immunology Disorders
Doctor
Dermatologist
Test Department
Genetics
Pre Test Information
Clinical History of Patient who is going for RAG2 Gene Omenn syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAG2 Gene Omenn syndrome NGS Genetic DNA Test gene RAG2
Test Details
The RAG2 gene is responsible for providing instructions for the production of a protein called recombination activating gene 2 (RAG2). This protein plays a crucial role in the immune system by helping to rearrange genetic material in immune cells to generate a diverse repertoire of antibodies and T-cell receptors.
Omenn syndrome is a rare genetic disorder that affects the immune system. It is characterized by severe combined immunodeficiency (SCID), which is a condition where the immune system is unable to function properly, leading to recurrent infections. Omenn syndrome is caused by mutations in genes involved in the development and function of immune cells.
NGS (Next-Generation Sequencing) is a high-throughput technology used to analyze DNA sequences. It allows for the simultaneous analysis of multiple genes or the entire genome, providing a comprehensive view of an individual’s genetic makeup. In the context of Omenn syndrome, NGS genetic testing can be used to identify mutations in the RAG2 gene or other genes associated with the disorder.
NGS genetic testing for Omenn syndrome involves obtaining a DNA sample from the individual, typically through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any mutations or variations in the RAG2 gene or other relevant genes. The results of the test can help in confirming a diagnosis of Omenn syndrome and provide information about the specific genetic mutation involved.
Genetic testing for Omenn syndrome can be useful for early diagnosis, allowing for prompt medical intervention and management. It can also help in providing genetic counseling to affected individuals and their families, as well as guiding potential treatment options.
| Test Name | RAG2 Gene Omenn syndrome Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for RAG2 Gene Omenn syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAG2 Gene Omenn syndrome NGS Genetic DNA Test gene RAG2 |
| Test Details |
The RAG2 gene is responsible for providing instructions for the production of a protein called recombination activating gene 2 (RAG2). This protein plays a crucial role in the immune system by helping to rearrange genetic material in immune cells to generate a diverse repertoire of antibodies and T-cell receptors. Omenn syndrome is a rare genetic disorder that affects the immune system. It is characterized by severe combined immunodeficiency (SCID), which is a condition where the immune system is unable to function properly, leading to recurrent infections. Omenn syndrome is caused by mutations in genes involved in the development and function of immune cells. NGS (Next-Generation Sequencing) is a high-throughput technology used to analyze DNA sequences. It allows for the simultaneous analysis of multiple genes or the entire genome, providing a comprehensive view of an individual’s genetic makeup. In the context of Omenn syndrome, NGS genetic testing can be used to identify mutations in the RAG2 gene or other genes associated with the disorder. NGS genetic testing for Omenn syndrome involves obtaining a DNA sample from the individual, typically through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any mutations or variations in the RAG2 gene or other relevant genes. The results of the test can help in confirming a diagnosis of Omenn syndrome and provide information about the specific genetic mutation involved. Genetic testing for Omenn syndrome can be useful for early diagnosis, allowing for prompt medical intervention and management. It can also help in providing genetic counseling to affected individuals and their families, as well as guiding potential treatment options. |
